Search
Disclaimer
Clicking the images or links will redirect you to a website hosted by BenchSci that provides third-party scientific content. Neither the content nor the BenchSci technology and processes for selection have been evaluated by us; we are providing them as-is and without warranty of any kind, including for use or application of the Thermo Fisher Scientific products presented.
Proteintech
ENOSF1 Recombinant Rabbit Monoclonal Antibody (240796D2)
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promotions']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.viewpromo']}}
{{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.promocode']}}: {{promo.promoCode}} {{promo.promoTitle}} {{promo.promoDescription}}. {{$productOrderCtrl.translations['antibody.pdp.commerceCard.promotion.learnmore']}}
产品信息
83769-2-RR
应用
建议稀释比
已发表文章
产品规格
种属反应
Human
宿主/亚型
Rabbit
/ IgG
Expression System
HEK293F
分类
Recombinant Monoclonal
类型
Antibody
克隆号
240796D2
抗原
ENOSF1 fusion protein Ag34665
偶联物
形式
Liquid
浓度
1 mg/mL
纯化类型
Protein A
保存液
PBS, pH 7.3, with 50% glycerol
内含物
0.02% sodium azide
保存条件
-20°C
运输条件
Wet ice
产品详细信息
Immunogen sequence: MVRGRISRL SVRDVRFPTS LGGHGADAMH TDPDYSAAYV VIETDAEDGI KGCGITFTLG KGTEVVVCAV NALAHHVLNK DLKDIVGDFR GFYRQLTSDG QLRWIGPEKG VVHLATAAVL NAVWDLWAKQ EGKPVWKLLV DMDPRMLVSC IDFRYITDVL TEEDALEILQ KGQIGKKERE KQMLAQGYPA YTTSCAWLGY SDDTLKQLCA QALKDGWTRF KVKVGADLQD DMRRCQIIRD MIGPEKTLMM DANQRWDVPE AVEWMSKLAK FKPLWIEEPT SPDDILGHAT ISKALVPLGI GIATGEQCHN RVIFKQLLQA KALQFLQIDS CRLGSVNENL SVLLMAKKFE IPVCPHAGGV GLCELVQHLI IFDYISVSAS LENRVCEYVD HLHEHFKYPV MIQRASYMPP KDPGYSTEMK EESVKKHQYP DGEVWKKLLP AQEN
靶标信息
DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
篇参考文献 (0)
您是否在文献中引用过该产品？请点击下方按钮邮件告知我们。
生物信息学
蛋白别名: Antisense RNA to thymidylate synthase; HSRTSBETA; L-fuconate dehydratase; Mitochondrial enolase superfamily member 1; rTS; rTS alpha; rTS beta
基因别名: ENOSF1; RTS; TYMSAS
UniProt ID: (Human) Q7L5Y1
Entrez Gene ID: (Human) 55556
